Stroke Patients' Preferences for an Exoskeleton for Lower Limb Rehabilitation Using the DCE Method (EXOPREF)
NCT ID: NCT06921031
Last Updated: 2025-04-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
60 participants
OBSERVATIONAL
2025-01-15
2025-12-31
Brief Summary
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Conditional logistic regression models will be used to define the preferences of the subjects.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* informed consent to participate in the study
* motor impairment secondary to stroke
* ability to answer the questionnaire with or without assistance from a relative or interviewer
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital, Brest
OTHER
Responsible Party
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Locations
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Chu Brest
Brest, , France
Centre de rééducation Kerpape
Ploemeur, , France
Countries
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Other Identifiers
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29BRC24.0363 - EXOPREF
Identifier Type: -
Identifier Source: org_study_id
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